ライフサイエンスコーパス: eminence

1 pulation derived from the lateral ganglionic eminence.

2 es in spontaneous GnRH release in the median eminence.

3 hin their birthplace, the lateral ganglionic eminence.

4 NK3R-expressing GnRH terminals in the median eminence.

5 y to the dorsal vagal complex and the median eminence.

6 ry vesicles in nerve terminals in the median eminence.

7 he release of GnRH from fibers in the median eminence.

8 ons with extensive projections to the median eminence.

9 GnRH terminal microenvironment in the median eminence.

10 es not enhance CRH storage within the median eminence.

11 of interneuron progenitors in the ganglionic eminence.

12 ate developmentally in the caudal ganglionic eminence.

13 nt and extension of GnRH axons to the median eminence.

14 ntricular zone and not the medial ganglionic eminence.

15 the internal and external zone of the median eminence.

16 ugh the tuberal hypothalamus into the median eminence.

17 ctions to the exterior portion of the median eminence.

18 rk of nerve fibers was present in the median eminence.

19 urons that derive from the medial ganglionic eminence.

20 d elicit papilla formation on the intermolar eminence.

21 r optic probe was placed over the hypothenar eminence.

22 the third ventricle to the caudal ganglionic eminence.

23 triatal boundary into the lateral ganglionic eminence.

24 2-1 leads to a loss of the medial ganglionic eminence.

25 derived from the embryonic medial ganglionic eminence.

26 activation of GnRH projections in the median eminence.

27 the cell body and DA secretion at the median eminence.

28 he internal and external zones of the median eminence.

29 migration from the MGE and caudal ganglionic eminence.

30 medial (MGE) or the caudal (CGE) ganglionic eminences.

31 ithelium but not medial or caudal ganglionic eminences.

32 as the medial, lateral, or caudal ganglionic eminences.

33 ), lateral (LGE) and caudal (CGE) ganglionic eminences.

34 ally along a medial path from the ganglionic eminences.

35 t populate the medial and lateral ganglionic eminences.

36 s originating in the more distant ganglionic eminences.

37 genetic evidence that the caudal ganglionic eminence, a distinct subpallial progenitor zone, contrib

38 is, Gsh2 expression in the medial ganglionic eminence after E10.5 may negatively regulate Nkx2.1 depe

39 the axons of the internal zone of the median eminence and a marked reduction in IL-6-like material in

40 pression of markers specific to the thalamic eminence and anterodorsal hypothalamus.

41 Thenar eminence and brain tissue oxygenation and side-stream da

42 IPe, arcuate nucleus of hypothalamus, median eminence and dorsal hypothalamic area in the diencephalo

43 generated from the ventral medial ganglionic eminence and dorsal preoptic area based on fate mapping

44 entrally by the Tbr-1-expressing prethalamic eminence and dorsally by the Gbx-2-expressing part of th

45 ory cells derived from the medial ganglionic eminence and few expressed VGAT, found in GABAergic inte

46 ne (BrdU) labeling in the lateral ganglionic eminence and frontal cortical neuroepithelium but not me

47 that are normally expressed in the thalamic eminence and in the anterodorsal hypothalamus in a porti

48 The lack of RFRP-3 fibers in the median eminence and of Fluoro-Gold uptake from the periphery im

49 y nuclei and in cell processes of the median eminence and pituitary stalk.

50 ogenitors in the embryonic medial ganglionic eminence and preoptic area preferentially develop electr

51 domains equivalent to the medial ganglionic eminence and rhombic lip, resembling the gnathostome bra

52 The lateral ganglionic eminence and rostral migratory stream developed normally

53 in cell death within the lateral ganglionic eminence and rostral migratory stream.

54 as well as the attachment between the tibial eminence and the anterior cruciate ligament, the latter

55 eoptic region, caudally with the prethalamic eminence and the prethalamus, and ventrally with the bas

56 e peak bone strain of the temporal articular eminence and the zygomatic arch both depend upon loading

57 the arcuate nucleus extending to the median eminence and throughout the periventricular zone of the

58 s are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic rudiments of

59 h as the olfactory primordium and ganglionic eminence and via a massive subpial granular layer that m

60 lx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the septum, resulting

61 haracterized the developing human ganglionic eminences and found that the subventricular zone (SVZ) e

62 K signaling in progenitors of the ganglionic eminences and had fewer SST(+) and VIP(+) interneurons.

63 arts of the hypothalamus, and the ganglionic eminences and their derivatives in the subpallial telenc

64 lar organs such as subfornical organ, median eminence, and area postrema.

65 ng choroid plexus, subfornical organ, median eminence, and area postrema.

66 fully complex human phenomena such as crime, eminence, and educational-vocational development, such a

67 of the ventral telencephalon, the ganglionic eminence, and migrate into the developing neocortex.

68 al interneuron migration from the ganglionic eminence, and reduced interneurons in the frontal and pa

69 um had hemorrhages in the cortex, ganglionic eminence, and thalamus, as well as abnormal vascular mor

70 pressed in the subfornical organ, the median eminence, and the area postrema.

71 esent within the arcuate nucleus, the median eminence, and the tuberal nucleus, and light immunostain

72 Z) is expressed in the developing ganglionic eminences, and their derivatives.

73 rate the cerebral cortex, but the ganglionic eminences are not affected.

74 d CVOs include the subfornical organ, median eminence, area postrema and choroid plexus, and accumula

75 us, and substantia nigra from the ganglionic eminence as development proceeds.

76 that are derived from the medial ganglionic eminence, as most studies have examined this interneuron

77 the cytoarchitectural features of the median eminence became disorganized with aging.

78 urons originate in the subpallial ganglionic eminences, but their developmental origins in humans are

79 in, reducing innervation of the adult median eminence by GnRH-positive neurites.

80 s lacking nNOS arises from caudal ganglionic eminence (CGE) progenitors.

81 nglionic eminence (MGE) or caudal ganglionic eminence (CGE) progenitors.

82 er, so far the role of the caudal ganglionic eminence (CGE), a posterior subpallial domain, in telenc

83 ganglionic eminence (LGE) caudal ganglionic eminence (CGE), and septum, including loss of GAD1 expre

84 ventral telencephalon, the caudal ganglionic eminence (CGE).

85 ns that originate from the caudal ganglionic eminence (CGE).

86 to derive mainly from the caudal ganglionic eminence (CGE).

87 from either the caudal or medial ganglionic eminences (CGE and MGE).

88 onic eminences (LGEs), and caudal ganglionic eminences (CGEs) between preterm-born [born on embryonic

89 The hypothalamic arcuate-median eminence complex (Arc-ME) controls energy balance, ferti

90 After median eminence compression to produce axonal injury, unilatera

91 ificantly different (P < or = 0.01) near the eminence crest, but joint load minimization was consiste

92 Our findings establish ganglionic eminence-dependent rules for early synaptic integration

93 , conditionally deleting Arx from ganglionic eminence derived neurons including cortical interneurons

94 ed in the prethalamus and lateral ganglionic eminence-derived corridor and on corticofugal axons, but

95 that Satb1 is required for medial ganglionic eminence-derived interneuron differentiation, connectivi

96 fferentiation of two major medial ganglionic eminence-derived interneuron populations and defines the

97 at O-LM cells parse into a caudal ganglionic eminence-derived subpopulation expressing 5-HT(3A) recep

98 ceptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3A)Rs.

99 entral neuronal specification and ganglionic eminence development in the Shh(N/-) telencephalon were

100 TCs arise from the dorsal lateral ganglionic eminence (dLGE) and migrate in the lateral migratory str

101 We found that dorsal lateral ganglionic eminence (dLGE)-derived olfactory bulb interneurons are

102 systemic administration of PRL-AB on median eminence DOPAC concentrations suggesting that the tonic

103 We measured oxygen consumption in the thenar eminence during brachial artery occlusion in sickle cell

104 recursors generated in the medial ganglionic eminence during embryogenesis.

105 ng cells, are born in the ventral ganglionic eminences during mid-gestation and then migrate tangenti

106 6ei) in embryonic day 13.5 medial ganglionic eminence (E13.5 MGE).

107 Very few fibers were observed in the median eminence, especially in the external zone.

108 The medial ganglionic eminence exhibited unique patterns of progenitor cell or

109 pus as well as lateral and medial ganglionic eminences exhibited a 20-30% reduction in mitotic neural

110 neurons that populate the lateral ganglionic eminence express different combinations of the homeobox-

111 ons originate from lateral/caudal ganglionic eminences, express the transcription factor FoxP2, fire

112 frontal arc, a moderately large juxtamastoid eminence, extremely large molars that become progressive

113 euroendocrine with projections to the median eminence for controlling anterior pituitary hormone secr

114 Although tibial eminence fractures are uncommon, their importance cannot

115 a gold standard modality in treating tibial eminence fractures, most studies agreed on several issue

116 progenitors of the dorsal lateral ganglionic eminence from Pax6 mutant Small Eye (Pax6(Sey/Sey)) mice

117 ncy of embryonic day 14.5 (E14.5) ganglionic eminence (GE) progenitors that grew into neurospheres in

118 lls isolated from the subpallium (ganglionic eminence) generate CalR(+) or GABA(+) cells, whereas thi

119 markers revealed that the caudal ganglionic eminence generated a greater proportion of cortical inte

120 the mammalian medial and lateral ganglionic eminences generated medium spiny neurons found in Area X

121 ilage, abnormal development of the articular eminence/glenoid fossa in the TMJ, and fusion of the art

122 t migrate ventrodorsally from the ganglionic eminences has not been explored in vivo.

123 rostral and caudal domains and a prethalamic eminence histogenetic domain in zebrafish.

124 termediate zones of the thalamus, ganglionic eminence, hypothalamus, and cortical preplate.

125 CVS did not alter CRH median eminence immunoreactivity, indicating that CVS does not

126 d midbrain, the optic chiasm, and the median eminence in the forebrain.

127 c interneurons originating in the ganglionic eminence in the ventral telencephalon.

128 arch and stresses of the temporal articular eminence in vitro, suggesting the need to verify whether

129 tical interneurons arise from the ganglionic eminences in the ventral telencephalon and migrate tange

130 interneurons are produced in the ganglionic eminences, including an enormous contribution from non-e

131 the volumes of basal ganglia and ganglionic eminence increase along with that of the whole brain, wh

132 eal gland, medial mammillary nucleus, median eminence, infundibular stem, periaqueductal gray, area p

133 Transplanting medial ganglionic eminence interneuron progenitors to introduce new GABAer

134 ed into the portal circulation at the median eminence, is known to prime downstream hormone release,

135 h is expressed only in the medial ganglionic eminence, is not.

136 e of the human SVZ at the lateral ganglionic eminence late in the second trimester of development (23

137 achiasmatic nucleus, arcuate nucleus, median eminence, lateral hypothalamic area, thalamus, hippocamp

138 tor zones in the pallium, lateral ganglionic eminence (LGE) and medial ganglionic eminence (MGE) in t

139 ubventricular zone of the lateral ganglionic eminence (LGE) at embryonic day 13.5 may underlie such d

140 ypes, particularly in the lateral ganglionic eminence (LGE) caudal ganglionic eminence (CGE), and sep

141 rt that activin A induces lateral ganglionic eminence (LGE) characteristics in nascent neural progeni

142 he size of the Tlx mutant lateral ganglionic eminence (LGE) from embryonic day 14.5 onward.

143 uronal progenitors of the lateral ganglionic eminence (LGE) in the ventral telencephalon.

144 The lateral ganglionic eminence (LGE) is known to give rise to striatal project

145 The embryonic lateral ganglionic eminence (LGE) is thought to be the site of origin of po

146 dh1a3), is reduced in the lateral ganglionic eminence (LGE) of Gsh2 mutants.

147 nal subtypes derived from lateral ganglionic eminence (LGE) progenitors at specific embryonic time po

148 f progenitor cells in the lateral ganglionic eminence (LGE), the neuroepithelial precursor of the neo

149 eurons (GABA INs), or the lateral ganglionic eminence (LGE), which generate GABA INs that normally mi

150 they acquire a subset of lateral ganglionic eminence (LGE)-specific properties at the expense of MGE

151 ways are generated in the lateral ganglionic eminence (LGE).

152 by their position in the lateral ganglionic eminence (LGE).

153 neurons derived from the lateral ganglionic eminence (LGE).

154 Ps from the lateral and/or caudal ganglionic eminences (LGE and CGE).

155 ls born in the lateral and medial ganglionic eminences (LGE and MGE) in 13.5-day-old mouse embryos.

156 enitors in the lateral and medial ganglionic eminences (LGE and MGE).

157 in the forebrain itself (lateral ganglionic eminence; LGE) starting at E12.5, suggesting a later rol

158 glionic eminences (MGEs), lateral ganglionic eminences (LGEs), and caudal ganglionic eminences (CGEs)

159 some MGE progenitors to a caudal ganglionic eminence-like, bipolar calretinin-expressing cell fate t

160 persistence of the dorsal lateral ganglionic eminence marker Sp8.

161 ed ventrally in the telencephalic ganglionic eminences (Mash1, Dlx2 and Gsh2) are upregulated cell au

162 tanycytes are stem cells and, in the median eminence, may be stimulated by diet to generate new neur

163 ed animals restored PC1 levels in the median eminence (ME) and the PVN to approximately the level fou

164 Placement of CFMEs in the median eminence (ME) near GnRH terminals allowed detection of b

165 e their neuroendocrine signals at the median eminence (ME) to control long-lasting pituitary hormone

166 ose axons project to the hypothalamic median eminence (ME) where they release gonadotropin-releasing

167 uid (CSF) barrier at the level of the median eminence (ME), a circumventricular organ (CVO) located i

168 ntral periventricular nucleus (AVPv), median eminence (ME), and dorsomedial portion of the ventromedi

169 dantly expressed in astrocytes of the median eminence (ME), and its enzymatic activity increases sele

170 irst OLPs originate in the medial ganglionic eminence (MGE) and anterior entopeduncular area (AEP) in

171 --including those from the medial ganglionic eminence (MGE) and OB--fail to generate neuroblasts with

172 Progenitor cells in the medial ganglionic eminence (MGE) and preoptic area (PoA) give rise to GABA

173 lencephalon, including the medial ganglionic eminence (MGE) and preoptic area.

174 neuron neurogenesis in the medial ganglionic eminence (MGE) and, more importantly, that estrogen trea

175 x2.1(+) progenitors in the medial ganglionic eminence (MGE) are misspecified such that they acquire a

176 c precursor cells from the medial ganglionic eminence (MGE) can migrate and differentiate into mature

177 tor cells derived from the medial ganglionic eminence (MGE) can reverse mechanical hypersensitivity i

178 Embryonic medial ganglionic eminence (MGE) cells transplanted into the adult brain c

179 d, a system modeling human medial ganglionic eminence (MGE) development, a critical ventral brain dom

180 neuron precursors from the medial ganglionic eminence (MGE) enhances GABAergic signaling in the brain

181 eloping telencephalon, the medial ganglionic eminence (MGE) generates many cortical and virtually all

182 The medial ganglionic eminence (MGE) gives rise to the majority of mouse foreb

183 glionic eminence (LGE) and medial ganglionic eminence (MGE) in the subpallium has been well studied;

184 GABAergic neurons from the medial ganglionic eminence (MGE) into adult mouse spinal cord ameliorates

185 r cells from the embryonic medial ganglionic eminence (MGE) into early postnatal neocortex generates

186 nterneurons from the mouse medial ganglionic eminence (MGE) into the adult mouse spinal cord complete

187 ventral telencephalon, the medial ganglionic eminence (MGE) is a major source of cortical interneuron

188 The medial ganglionic eminence (MGE) is an embryonic forebrain structure that

189 Young neurons born in the medial ganglionic eminence (MGE) migrate a long distance dorsally, giving

190 mosaic elimination in the medial ganglionic eminence (MGE) of Smo, a key effector of SHH signaling,

191 inate primarily within the medial ganglionic eminence (MGE) of the subcortical telencephalon, whereas

192 ting cells by lineage from medial ganglionic eminence (MGE) or caudal ganglionic eminence (CGE) proge

193 NGCs are both derived from medial ganglionic eminence (MGE) progenitors under control of the transcri

194 ajor subtypes generated by medial ganglionic eminence (MGE) progenitors.

195 ted in a partial rescue of medial ganglionic eminence (MGE) properties, including interneuron migrati

196 ntricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice causes moderate or s

197 N subtypes derive from the medial ganglionic eminence (MGE), a transient ventral telencephalic struct

198 nic structure known as the medial ganglionic eminence (MGE), but how the remarkable diversity is spec

199 euron progenitors from the medial ganglionic eminence (MGE), can overcome the mechanical hypersensiti

200 interneurons, derived from medial ganglionic eminence (MGE), is implicated in disorders of learning a

201 ing on the mouse embryonic medial ganglionic eminence (MGE), the major birthplace for CINs, and on MG

202 lation was examined in the medial ganglionic eminence (MGE), the major source of PV interneurons in m

203 cursors from the embryonic medial ganglionic eminence (MGE), the source of neocortical parvalbumin- (

204 erneurons originate in the medial ganglionic eminence (MGE), where the signaling molecule sonic hedge

205 not by progenitors in the medial ganglionic eminence (MGE), which generate cortical GABAergic intern

206 oring tdTomato-fluorescent medial ganglionic eminence (MGE)-derived cortical GABAergic interneurons w

207 terestingly, compared with medial ganglionic eminence (MGE)-derived cortical interneuron populations,

208 Medial ganglionic eminence (MGE)-derived GABAergic cortical interneurons (

209 erentiation of a subset of medial ganglionic eminence (MGE)-derived neurons, but are dispensable for

210 alic excitatory neurons or medial ganglionic eminence (MGE)-like inhibitory neurons.

211 ferentiation of hPSCs into medial ganglionic eminence (MGE)-like progenitors and their maturation int

212 subpallium, including the medial ganglionic eminence (MGE).

213 erneurons generated in the medial ganglionic eminence (MGE).

214 t primarily resides in the medial ganglionic eminence (MGE).

215 g those originating in the medial ganglionic eminence (MGE).

216 e neurons derived from the medial ganglionic eminence (MGE).

217 s from embryonic medial or caudal ganglionic eminence (MGE, CGE) were made in a well-characterized mo

218 embryo from the medial or caudal ganglionic eminences (MGE and CGE).

219 from either the medial or caudal ganglionic eminences (MGE and CGE).

220 ng of the mouse medial and caudal ganglionic eminences (MGE and CGE, respectively), from which most c

221 ncephalon: the medial and lateral ganglionic eminences (MGE and LGE).

222 euronal progenitors in the medial ganglionic eminences (MGEs), lateral ganglionic eminences (LGEs), a

223 as examined: embryonic neocortex, ganglionic eminence, midbrain, retina, hindbrain, and spinal cord;

224 arise from the medial and lateral ganglionic eminences, morphologically distinct structures found in

225 aring adeno-associated virus into the median eminence of adult GnRH-Cre mice resulted in the selectiv

226 Our results highlight the pre-eminence of cis-acting variants on transcription factor

227 These results call into question the pre-eminence of escape as the primary advantage of dispersal

228 odendrogenesis, within the medial ganglionic eminence of Nkx2.1 mutants, the early expression of PDGF

229 and resembled structures seen in the median eminence of rats.

230 GnRH release detected by FSCV in the median eminence of slices from adults with previous reports of

231 T(H)-17 lineage appeared to supplant the pre-eminence of T(H)1 cells in promoting autoimmunity, the n

232 In addition, unlike in the ganglionic eminence of the embryonic forebrain where Olig2 is mostl

233 Pe neurons derive from the medial ganglionic eminence of the embryonic subpallium and express the tra

234 elivered to a central location on the thenar eminence of the hand.

235 ted by infusion of letrozole into the median eminence of the hypothalamus.

236 a contingent of neurons from the ganglionic eminence of the telencephalon migrate to the dorsal thal

237 ar neurons has been observed, the ganglionic eminence of the telencephalon.

238 nterneurons that originate in the ganglionic eminence of the ventral forebrain and incorporate into t

239 c neurons and originates from the ganglionic eminence of the ventral forebrain.

240 al investigations, although recently the pre-eminence of this system in nicotine dependence has been

241 These results confirm the pre-eminence of type 1 fimbriae, establish the importance of

242 r surrounding microenvironment in the median eminence of young (4-5 months) and old (22-24 months) ov

243 rons within the medial and caudal ganglionic eminences of the developing telencephalon.

244 mulation applied independently to the thenar eminence on each hand and also to bilateral (simultaneou

245 of the lateral septum, but not in the median eminence or in the arcuate nucleus, even though both MOR

246 ignificantly higher than the adult articular eminence (p < 0.05).

247 othalamic area (MBA), arcuate nucleus/median eminence, paraventricular nuclei and piriform cortex.

248 the caudate nucleus adjoining the ganglionic eminence, potentially a waiting compartment.

249 n precursors in the developing telencephalic eminences predicts the intrinsic physiological propertie

250 erned to NKX2.1-expressing medial ganglionic eminence progenitors by simple treatment with sonic hedg

251 mine whether hypocretin modulates the median eminence-projecting proopiomelanocortin (POMC) neurons i

252 onpainful punctate stimulation of the thenar eminence provoked more diffuse activity but was still ip

253 m the medial basal hypothalamus (MBH)/median eminence region (S-ME) is essential for normal reproduct

254 es, an ependymoglial cell type of the median eminence, regulate LHRH release during the estrous cycle

255 nhibitory neurons from the medial ganglionic eminence reinstate ocular dominance plasticity in adult

256 ch in Nkx2.1 expression, and the prethalamic eminence, rich in Tbr1 expression.

257 joint load minimization was consistent with eminence shape for x < 3.0 mm.

258 ypothesis that temporomandibular joint (TMJ) eminence shapes develop ideally to minimize joint loads.

259 dict, and jaw-tracking data used to measure, eminence shapes.

260 only in the subfornical organ and the median eminence, situated outside the blood brain barrier, but

261 GABA neurons identified by antidromic median eminence stimulation.

262 the cortical anlage (CTXOE03) and ganglionic eminence (STROC05), as well as an adult EC line (D3) der

263 he lateral (LGE) and medial (MGE) ganglionic eminences, subpallial embryonic structures, is required

264 us, amygdala, thalamus, hypothalamus, medium eminence, substantia nigra, ventral tegmental area, ocul

265 , in GABAergic nerve terminals in the median eminence suggested that rather than a functional redunda

266 e in GABAergic nerve terminals in the median eminence suggests that only the non-GABAergic dopamine n

267 he cortex, most stem cells in the ganglionic eminence SVZ did not maintain radial fibers or orientati

268 s, most of which originate in the ganglionic eminences, take distinct tangential migratory trajectori

269 g genetic fate mapping, we found that median eminence tanycytes generate newborn neurons.

270 within the infundibular stalk/caudal median eminence, termed here gamma tanycytes, and a subset of c

271 to neural progenitor cells in the ganglionic eminence that are fated to differentiate into GABAergic

272 omologue of the mammalian lateral ganglionic eminence (the adult caudatoputamen in mammals).

273 homologue of the mammalian medial ganglionic eminence (the adult pallidum in mammals).

274 f cells from the embryonic medial ganglionic eminence (the major origin of cerebral cortical interneu

275 In the medial ganglionic eminence, the NKX2-1 transcription factor controls regio

276 ellular level, we show that, similar to bone eminences, the patella is formed secondarily by a distin

277 eniculate nucleus from the caudal ganglionic eminence, there is no obvious new source of proliferatin

278 pting specification of the medial ganglionic eminence through loss of Nkx2.1 homeobox function deplet

279 migration from the dorsal lateral ganglionic eminence through maturity.

280 telencephalon (lateral and medial ganglionic eminences) through loss of Dlx1/2 homeobox function bloc

281 namic variables and also cerebral and thenar eminence tissue oxygenation and side-stream dark-field i

282 Median eminence tissues were freeze-plunge embedded and serial

283 hat the GnRH neuron projection to the median eminence to control pituitary hormone secretion possesse

284 rneurons migrate from the ventral ganglionic eminence to the cerebral cortex within several migratory

285 ransported in varicose fibres via the median eminence to the posterior pituitary gland.

286 ration from the medial and caudal ganglionic eminences to the cerebral cortex in slice preparations o

287 ate tangentially from the ventral ganglionic eminences to the developing cortex.

288 from their place of birth in the ganglionic eminences to their place of terminal differentiation in

289 ors normally found in the lateral ganglionic eminence, to prevent precocious differentiation and depl

290 om their generation in the medial ganglionic eminence up to their settlement in the AC, express two c

291 rogenitors are located within the ganglionic eminences, using Dlx5/6-Cre-ires-EGFP (Dlx5/6-CIE) mice.

292 Enforced collapse of ganglionic eminence vessels and resultant periventricular neural ap

293 se in target brain regions and in the median eminence via a direct inhibition of vGluT2-GnRH neurons.

294 rs located in the ventral lateral ganglionic eminence (vLGE).

295 ne strain of the juvenile temporal articular eminence was significantly higher than the adult articul

296 ced secretion of dopamine (DA) at the median eminence was strongly blunted during lactation, at least

297 wn to innervate the middle finger and thenar eminence were also transected.

298 those that project their axons to the median eminence, were robustly activated by hypocretin in a dos

299 icular-subventricular zone of the ganglionic eminences, whereas at midgestation (20 GW), they were al

300 aired proliferation in the medial ganglionic eminence without grossly altering differentiated fate.